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Spots Global Cancer Trial Database for A Prospective Study for the Assessment of Recurrence Risk in Stage II Colon Cancer Patients Using ColoPrint

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Trial Identification

Brief Title: A Prospective Study for the Assessment of Recurrence Risk in Stage II Colon Cancer Patients Using ColoPrint

Official Title: A Prospective Study for the Assessment of Recurrence Risk in Stage II Colon Cancer Patients Using ColoPrint

Study ID: NCT00903565

Conditions

Colon Cancer

Interventions

Study Description

Brief Summary: The aim of this study is to enroll 785 eligible stage II colon cancer patients in order to validate the performance of ColoPrint in estimating 3-year relapse rate. Secondary objectives include comparing the objective risk assessment results from the prognostic profile (ColoPrint) to both the risk assessment based on the ASCO criteria, as well as the Investigator's independent assessment. As this is the first prospective study of ColoPrint, this study will also address the logistics and quality assurance of using ColoPrint in clinical practice. Patient treatment is at the discretion of the physician, adhering to National Comprehensive Cancer Network (NCCN)-approved regimens or a recognized alternative. The enrollment period will be 6 years. It is expected that 1800 to 2400 patients will be enrolled in order to obtain 785 analysable stage II samples from eligible patients. Approximately 25-35 clinical sites will be involved worldwide. The statistical analysis will be performed by Agendia and an independent research institute or hospital. Study Design Extension Study: This will be a prospective study to measure the impact of ColoPrint on adjuvant treatment in stage 2 colorectal cancer patients. After surgery the tumor sample will be shipped in RNA Retain to Agendia. The online Clinical Report Form (CRF) 0 will be completed to document if the patient fulfils the inclusion criteria. Baseline clinical data and the patient and physician chemotherapy intention, patient's perceived recurrence risk and decisional conflict without knowing the ColoPrint result will be entered in CRF 1. After completion of CRF1 the ColoPrint result is released. CRF2 will be completed after the final treatment decision has been made. This CRF will capture the patient and physician chemotherapy intention, patient's perceived recurrence risk and decisional conflict, impact of ColoPrint and the actual treatment the patient will receive. CRF3 will be completed 12 months after enrolment and will capture the patient status, patient's perceived recurrence risk and decisional conflict. CRF4 and 5 will be completed 3 and 5 years after surgery and will capture the patient status. A sample size of 210 stage 2 colon cancer patients is required to detect a 10% overall treatment change (5% significance and 90% power). Reporting of the Results: Blinded Study; The ColoPrint results will not be reported to the physician and/or patient at the time of enrolment. All samples will be stored in a freezer until 550-575 eligible stage II patients have been enrolled. Samples will then be analyzed in one batch in a blinded fashion from the clinical results. Extension Study; The ColoPrint results will be reported to the physician and patient after CRF1 has been completed.

Detailed Description: Primary Objective • To validate the performance of ColoPrint in estimating the 3-year relapse rate in patients with stage II colorectal cancer. Secondary Objectives • To assess the feasibility of using the ColoPrint test in the clinical setting. * To compare the risk assessment in stage II patients using the ColoPrint profile vs a clinical risk assessment based on 1) Investigator's assessment of risk and 2) ASCO high-risk recommendations (T4 lesions, perforation / obstruction, inadequate node sampling (less than 12 nodes) or poorly differentiated histology). * To establish the proportion of low-risk and high-risk ColoPrint profiles in stage II colorectal cancer patients in various countries. * To investigate therapy as a potential confounding factor for ColoPrint results. * To assess the performance of ColoPrint in estimating the 3-year relapse rate in patients with stage III colorectal cancer. * To compare the performance of ColoPrint vs the clinical risk assessment in estimating the 5-year relapse rate. * Assess the impact of ColoPrint on adjuvant chemotherapy treatment decisions in stage 2 colorectal cancer patients * Compare the ColoPrint results from fresh RNARetain colorectal tumor specimens to the matched formalin-fixed paraffin-embedded tissue (FFPE) colon tumor specimens for concordance.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Glendale Memorial Hospital, Glendale, California, United States

South Orange County Surgical Medical Group, Laguna Hills, California, United States

Long Beach Memorial Medical Center, Long Beach, California, United States

Sutter Roseville Medical Center /Research, Roseville, California, United States

Sutter Cancer Center, Sacramento, California, United States

UC Davis Cancer Center, Sacramento, California, United States

Scripps Cancer Center, San Diego, California, United States

University of Colorado Cancer Center, Aurora, Colorado, United States

Yale Cancer Center, New Haven, Connecticut, United States

Georgetown University Hospital, Washington, District of Columbia, United States

University of Miami, Miami, Florida, United States

Atlanta Colon and Rectal Surgery, Riverdale, Georgia, United States

Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York, United States

Wake Forest University, Winston-Salem, North Carolina, United States

Ohio State University, Columbus, Ohio, United States

MD Anderson Cancer Center, Houston, Texas, United States

Franciscan Research Center, Tacoma, Washington, United States

Landeskrankenhaus Feldkirch, Feldkirch, , Austria

Krankenhaus der Elisabethinen, Linz, , Austria

Medical University of Vienna, Vienna, , Austria

University of Hong Kong/ Queen Mary Hospital, Hong Kong, , China

Odense Universitetshospital, Odense, , Denmark

CRLC Val d'Aurelle-Paul Lamarque, Montpellier, , France

Klinikum Rechts Der Isar, Munich, , Germany

Matsuda Hospital, Hamamatsu, , Japan

Medisch Centrum Alkmaar, Alkmaar, , Netherlands

Medisch Spectrum Twente, Enschede, , Netherlands

Westfriesgasthuis, Hoorn, , Netherlands

LUMC, Leiden, , Netherlands

Vall d' Hebron University Hospital, Barcelona, , Spain

IDIBELL Institut Catala d'Oncologia (ICO), L'Hospitalet de Llobregat, , Spain

Immunology Akademiska sjukhuset/ University Hospital, Uppsala, , Sweden

Kantonsspital Baden, Baden, , Switzerland

Norfolk and Norwich University Hospital, Norwich, , United Kingdom

University of Oxford, Oxford, , United Kingdom

Contact Details

Name: Ramon Salazar, MD

Affiliation: Institut Català D´Oncologia, L'Hospitalet Barcelona

Role: PRINCIPAL_INVESTIGATOR

Name: John L Marshall, MD

Affiliation: Chief, Division of Hematology/Oncology, Georgetown University Hospital Washington

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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